ライフサイエンスコーパス: acid phosphatase

1 , TRAF6, cathepsin K, and tartrate-resistant acid phosphatase.

2 the nuclear entry of lipin 1, a phosphatidic acid phosphatase.

3 m of activated PMN by secreting at least one acid phosphatase.

4 ng peptide fragment of the protein prostatic acid phosphatase.

5 alkaline phosphatase, or tartrate-resistant acid phosphatase.

6 hematoxylin and eosin or tartrate-resistant acid phosphatase.

7 ith hematoxylin-eosin and tartrate-resistant acid phosphatase.

8 stimulate T-cell immunity against prostatic acid phosphatase.

9 hese genes is PHO5, which encodes a secreted acid phosphatase.

10 strated by the underglycosylation of surface acid phosphatase.

11 cts, such as androgen receptor and prostatic acid phosphatase.

12 served in the structural homologue prostatic acid phosphatase.

13 ession of the target gene tartrate-resistant acid phosphatase.

14 rvation-induced gene (LePS2) representing an acid phosphatase.

15 rosophila homologs of mammalian phosphatidic acid phosphatase.

16 asein was then dephosphorylated using potato acid phosphatase.

17 oclasts was determined by tartrate-resistant acid phosphatase.

18 ase, NT5E, and to a lesser extent, prostatic acid phosphatase.

19 as 10(-10)) to bacterial class A nonspecific acid phosphatases.

20 and is the prototype of class C nonspecific acid phosphatases.

21 hanistic similarity to iron-dependent purple acid phosphatases.

22 phytases, which were classified as histidine acid phosphatases.

23 ich contains a number of magnesium-dependent acid phosphatases.

24 of the P substrate spectrum based on purple acid phosphatases.

25 ologue, murine Kv3.1b, are both modulated by acid phosphatases.

26 ge disequilibrium block containing the ACP1 (acid phosphatase 1) gene, a gene whose expression is sig

27 amage-binding protein 2 (DDB2) and lysosomal acid phosphatase 2 (ACP2) genes.

28 e protein (VCIP), also known as phosphatidic acid phosphatase 2b (PAP2b), in a functional assay of an

29 growth factor (PDGF)-beta, and phosphatidic acid phosphatase 2b (PPAP2B).

30 ins in different tissues, led us to identify acid phosphatase 5 (ACP5) as a candidate for the enzyme

31 of target genes like cathepsin K (Ctsk) and acid phosphatase 5 (Acp5) during osteoclast differentiat

32 , cathepsin K (Cstk), and tartrate-resistant acid phosphatase 5 (TRAP) with receptor activator of NF-

33 erine/threonine protein phosphatases, purple acid phosphatases, 5'-nucleotidase, and DNA repair enzym

34 vo bone resorption marker tartrate-resistant acid phosphatase 5b (TRACP 5b).

35 e phosphatase (B-ALP) and tartrate-resistant acid phosphatase 5b (TRAP-5b), and calcium and alveolar

36 d by an increase in serum Tartrate-resistant acid phosphatase 5b (TRAP5b) levels.

37 Even though tartrate-resistant acid phosphatase 5b was expressed, proteolytic activatio

38 -terminal propeptide, and tartrate-resistant acid phosphatase 5b were associated with higher odds of

39 I collagen) and TRACP-5b (tartrate-resistant acid phosphatase 5b).

40 N-terminal propeptide, or tartrate-resistant acid phosphatase 5b; these values corresponded to the up

41 evels of human OPG-Fc and tartrate-resistant acid phosphatase-5b (TRAP-5b) were measured throughout t

42 The N-terminal portion of the M. catarrhalis acid phosphatase A (MapA) was most similar (the BLAST pr

43 om PMN through expression of an unidentified acid phosphatase (ACP).

44 Hence, the acid phosphatases AcpA, AcpB, and AcpC do not contribute

45 hu S4 the pathogenic roles of three distinct acid phosphatases, AcpA, AcpB, and AcpC, that are most c

46 se-1-phosphate (G1P) adsorbed on goethite by acid phosphatase (AcPase) can be of the same order of ma

47 Electron microscopic localization of acid phosphatase (AcPase) revealed that AcPase started t

48 diates the transport of ESCP and the soluble acid phosphatase (AcPh) to the PVs.

49 of this study was to delete the four primary acid phosphatases (Acps) from Francisella novicida and e

50 nd tartrate-sensitive and tartrate-resistant acid phosphatase activities and influences the appearanc

51 and human macrophages, despite decreases in acid phosphatase activities by as much as 95%.

52 ot in dolichyl monophosphate or phosphatidic acid phosphatase activities in microsomal fractions.

53 alcium release or uptake, tartrate-resistant acid phosphatase activity (marker for osteoclasts), alka

54 unrecognized link between tartrate-resistant acid phosphatase activity and interferon metabolism and

55 ucture, but resulted in complete loss of its acid phosphatase activity as well as its anti-insect act

56 Pae SurEalpha has optimal acid phosphatase activity at temperatures above 90 degre

57 ne in M. catarrhalis strain O35E reduced the acid phosphatase activity expressed by this organism, an

58 Acid phosphatase activity in the highly infectious intra

59 n Escherichia coli confirmed the presence of acid phosphatase activity in the MapA protein.

60 e acid phosphatase domain in MapA eliminated acid phosphatase activity in the recombinant MapA protei

61 s demonstrated that in the disruption strain acid phosphatase activity is expressed constitutively, a

62 es (PBL) and enhanced the respiratory burst, acid phosphatase activity, chemotactic activity, and gen

63 which contributes most of the F. tularensis acid phosphatase activity, is secreted into the culture

64 n (DeltaABCH) resulted in a 90% reduction in acid phosphatase activity.

65 of an autotransporter protein that expresses acid phosphatase activity.

66 its defense function is correlated with its acid phosphatase activity.

67 tase, but rather may regulate nonrepressible acid phosphatase activity.

68 assessed by staining for tartrate-resistant acid phosphatase activity.

69 gene product accounts for a majority of the acid phosphatase activity.

70 cuolar H(+)-ATPase; TRAP, tartrate-resistant acid phosphatase; alphaMEM D10, minimal essential media,

71 tions and increased serum tartrate-resistant acid phosphatase and 25-hydroxyvitamin D concentrations

72 They express prostatic acid phosphatase and androgen receptors and require seve

73 L-specific genes, such as tartrate-resistant acid phosphatase and immunoreceptor OCL-associated recep

74 role of LdRab1 in the secretion of secretory acid phosphatase and Ldgp63 in Leishmania.

75 ecific differences in the activities of both acid phosphatase and nitrate reductase.

76 Tartrate-resistant acid phosphatase and osteocalcin were used to identify o

77 HAD1 is a functional HAD protein having both acid phosphatase and phytase activities, it showed littl

78 arley, we found that the dynamics with which acid phosphatase and protease activities changed were di

79 involved in phosphate acquisition (the Pho1 acid phosphatase and the phosphate transporter SPBC8E4.0

80 steoclasts that expressed tartrate-resistant acid phosphatase and were capable of resorption.

81 105-kDa protein that has similarity to both acid phosphatases and autotransporters.

82 , 2, and 3 are Mg(2+)-dependent phosphatidic acid phosphatases and catalyze the penultimate step of t

83 Finally, the structures suggest that class B acid phosphatases and CCAPs share a common strategy for

84 tularensis and prototype of a superfamily of acid phosphatases and phospholipases C.

85 This architecture is unique among acid phosphatases and resembles that of alkaline phospha

86 roteinase 9, cathepsin K, tartrate-resistant acid phosphatase, and carbonic anhydrase II in bone marr

87 of the HCL markers CD25, tartrate-resistant acid phosphatase, and cyclin D1, smoothening of leukemic

88 eceptors for AGEs (RAGE), tartrate-resistant acid phosphatase, and proliferating cell nuclear antigen

89 receptor for AGEs (RAGE), tartrate-resistant acid phosphatase, and proliferating cell nuclear antigen

90 cluding ribonuclease, phosphodiesterase, and acid phosphatase; and (e) steady-state mRNA levels of ph

91 At the community level, potential acid phosphatase (AP) activity of ECM fungal root tips f

92 ong these is secretion of copious amounts of acid phosphatase (APase).

93 Plants secrete acid phosphatases (APases) into the apoplastic space, wh

94 hate is removed from NMN in the periplasm by acid phosphatase (AphA), and the produced nicotinamide r

95 ogether, this body of evidence suggests that acid phosphatases are general regulatory partners of Sha

96 Bacterial acid phosphatases are thought to play a major role in th

97 d expression of tartrate-sensitive prostatic acid phosphatase as a broadly acting ectonucleotidase.

98 red ex vivo with recombinant mouse prostatic acid phosphatase as the target neoantigen.

99 rmation was determined by tartrate resistant acid phosphatase assay.

100 d immunosorbent assay and tartrate-resistant acid phosphatase assay.

101 n this study, we identified ACPT (testicular acid phosphatase) biallelic mutations causing non-syndro

102 s not the structural gene for nonrepressible acid phosphatase, but rather may regulate nonrepressible

103 ficantly inhibits the secretion of secretory acid phosphatase by Leishmania.

104 proteolytic peptide fragments from prostatic acid phosphatase can form amyloid fibrils termed SEVI (s

105 Histidine acid phosphatases catalyze the transfer of a phosphoryl

106 eceptor, but they express tartrate-resistant acid phosphatase, cathepsin K, and beta(3) integrin, sug

107 ted transcription factor, tartrate-resistant acid phosphatase, cathepsin K, and beta3 integrin.

108 P4 is also the prototype of class C acid phosphatases (CCAPs), which are nonspecific 5',3'-n

109 rophosphorylation was decreased in prostatic acid phosphatase cDNA-transfected stable subclones of C-

110 spho-monoesterase, i.e. a tartrate-resistant acid phosphatase (Cl MAcP) was also found to be up-expre

111 main fold similar to that of human prostatic acid phosphatase, consisting of an alpha/beta core domai

112 Pharmacological inactivation of acid phosphatases could potentially help in the treatmen

113 -growing cells by cellular form of prostatic acid phosphatase (cPAcP) expression, a negative growth r

114 Cellular prostatic acid phosphatase (cPAcP), an authentic tyrosine phosphat

115 Thus, the Francisella acid phosphatases cumulatively play an important role in

116 o measure and characterise the activities of acid phosphatase, cysteine protease and nitrate reductas

117 in conjunction with immunohistochemistry and acid phosphatase cytochemistry to better define the bact

118 orters upon proteolytic cleavage, as well as acid phosphatase cytochemistry to identify which endocyt

119 ein tyrosine phosphatase, cellular prostatic acid phosphatase, decreased correspondingly in those cel

120 dAMP, and BPQ-dCMP adducts were confirmed by acid phosphatase dephosphorylation of the BPQ-nucleotide

121 FtHAP and human prostatic acid phosphatase differ in the orientation of the crucia

122 phosphatase was consistent with phosphatidic acid phosphatase domain containing 2 (PPAPDC2), an uncha

123 (H233A) in the predicted active site of the acid phosphatase domain in MapA eliminated acid phosphat

124 Here, we use simulations of purple acid phosphatase evolution to show that amino acid prope

125 nsgenic construct using a tartrate-resistant acid phosphatase exon 1C promoter to drive expression of

126 lp understand the catalytic mechanism of the acid phosphatase family.

127 ologous dendritic cells expressing prostatic acid phosphatase (for prostate cancer) or with autologou

128 fs in known alkaline phosphatases and purple acid phosphatase from red kidney bean shows that most of

129 The histidine acid phosphatase from the category A pathogen Francisell

130 AcpA is a respiratory burst-inhibiting acid phosphatase from the Centers for Disease Control an

131 with MITF to activate the tartrate-resistant acid phosphatase gene promoter dependent on Ser(307).

132 infection (SEVI) originating from prostatic acid phosphatase greatly increase XMRV infections of pri

133 e four Acps (AcpA, AcpB, AcpC, and histidine acid phosphatase [Hap]) in an F. novicida strain (DeltaA

134 ssed by histomorphometry, tartrate-resistant acid phosphatase histoenzymology, and cathepsin B (CATB)

135 uencing of ACP5, encoding tartrate-resistant acid phosphatase, identified biallelic mutations in each

136 ar factor kappa beta, and tartrate-resistant acid phosphatase immunostaining.

137 to PHOG, a possible phosphate nonrepressible acid phosphatase in Aspergillus nidulans.

138 volution of a phosphate starvation-inducible acid phosphatase in C. glabrata relative to most yeast s

139 the unexpected mitotic induction of the PHO5 acid phosphatase in rich medium requires the transcripti

140 In the acid phosphatase inducible PHO5 gene, we find that there

141 y heparin and spermine but not by either the acid phosphatase inhibitors citrate and tartrate or the

142 Lipin-1 is a Mg(2+)-dependent phosphatidic acid phosphatase involved in the de novo synthesis of ph

143 des a class of Mg(2+)-dependent phosphatidic acid phosphatases involved in the de novo synthesis of p

144 trolled activation of hydrolytic activity of acid phosphatase is successfully demonstrated.

145 se (TMPase, also known as fluoride-resistant acid phosphatase) is a classic histochemical marker of s

146 of degradative enzymes, including lysosomal acid phosphatase (LAP) and cathepsin B, are elevated, an

147 n phosphate transporter (LaPT1) and secreted acid phosphatase (LaSAP1) promoter-reporter genes when t

148 gh-affinity Pi transporters); LePS2 (a novel acid phosphatase); LePS3 and TPSI1 (novel genes); and PA

149 body mass index, race, Gleason score, stage, acid phosphatase level, prostatectomy history, and nodal

150 Mutants lacking either the known secreted acid phosphatases, lipases, phospholipase C, lysophospho

151 activator of the ER-associated phosphatidic acid phosphatase lipin that promotes synthesis of major

152 d dephosphorylates the mammalian phospatidic acid phosphatase, lipin.

153 d reactive substances, acetylcholinesterase, acid phosphatase), no significant effects were detected.

154 that inactivation of Ned1, the phosphatidic acid phosphatase of the lipin family, by CDK phosphoryla

155 results and on sequence alignment to purple acid phosphatases of known structure.

156 que externally oriented, tartrate-resistant, acid phosphatase on its surface membrane.

157 orphology was analyzed in tartrate-resistant acid phosphatase or F-actin-stained samples, and bone re

158 1b, the osteoclast marker tartrate-resistant acid phosphatase, or carbonic anhydrase II.

159 Human prostatic acid phosphatase (PAcP) is a prostate epithelium-specifi

160 Human prostatic acid phosphatase (PAcP) is a prostate epithelium-specifi

161 regulated by the cellular form of prostatic acid phosphatase (PAcP), a prostate-unique protein tyros

162 absent on vacuoles lacking the phosphatidic acid phosphatase Pah1, which also lack Ypt7, the phospha

163 ined much less Mg(2+)-dependent phosphatidic acid phosphatase (PAP) activity than tissues from wild t

164 unized with a DNA vaccine encoding prostatic acid phosphatase (PAP) and a trans-vivo delayed-type hyp

165 Prostatic acid phosphatase (PAP) and ecto-5'-nucleotidase (NT5E) h

166 nts of the abundant semen proteins prostatic acid phosphatase (PAP) and semenogelins form amyloid fib

167 and Ingenuity Systems) identified prostatic acid phosphatase (PAP) as an enzyme overexpressed in pro

168 LPIN1, which encodes lipin-1, a phosphatidic acid phosphatase (PAP) controlling the rate-limiting ste

169 enotype was caused by activation of a purple acid phosphatase (PAP) gene, AtPAP15, which contains a d

170 e X-ray crystal structure of human prostatic acid phosphatase (PAP) in complex with a phosphate ion h

171 Prostatic acid phosphatase (PAP) is a prostate tumor antigen.

172 Prostatic acid phosphatase (PAP) is expressed in nociceptive dorsa

173 Prostatic acid phosphatase (PAP) is just such an Ag that is expres

174 Lipin 2 is a phosphatidic acid phosphatase (PAP) responsible for the penultimate s

175 odology is able to report on human prostatic acid phosphatase (PAP), a tumor marker, with a limit of

176 al to the transmembrane isoform of prostatic acid phosphatase (PAP), an enzyme with unknown molecular

177 ostate-specific antigen (PSA), and prostatic acid phosphatase (PAP), and is derived from the highly a

178 pain may be mediated by decreased prostatic acid phosphatase (PAP), as PAP levels are markedly reduc

179 tion and, as a Mg(2+)-dependent phosphatidic acid phosphatase (PAP), is a key enzyme in the biosynthe

180 using Sipuleucel-T, an autologous prostatic acid phosphatase (PAP)-loaded dendritic cell immunothera

181 to-5'-nucleotidase (NT5E, CD73) or prostatic acid phosphatase (PAP, ACPP).

182 HT-1, while its mammalian homolog, prostatic acid phosphatase (PAP; also known as ACPP-201) stably as

183 (a proteolytic cleavage product of prostatic acid phosphatase, PAP(248-286)).

184 PhoD is most closely related to purple acid phosphatases (PAPs) with both types of enzyme conta

185 gy to members of the phosphoglycerate mutase/acid phosphatase (PGM/AcP) family of enzymes, with resid

186 st the gene encoding a phosphate-repressible acid phosphatase (PHO5) present in many yeasts including

187 port studies on a native E. coli periplasmic acid phosphatase, phytase (AppA), which contains three c

188 Thus, Francisella acid phosphatases play a major role in intramacrophage s

189 TRAP (tartrate-resistant acid phosphatase)-positive osteoclasts appeared on day 2

190 tein, along with elevated tartrate-resistant acid phosphatase-positive (TRAP+) OCs and alveolar bone

191 in (IL)-1beta levels, and tartrate-resistant acid phosphatase-positive (TRAP+) osteoclast numbers wer

192 d with significantly more tartrate-resistant acid phosphatase-positive (TRAP+) osteoclasts.

193 pletion of PDGF-BB in the tartrate-resistant acid phosphatase-positive cell lineage show significantl

194 number of multinucleated tartrate-resistant acid phosphatase-positive cells along the alveolar bone

195 osteoclasts with reduced tartrate-resistant acid phosphatase-positive cells and dentine resorption c

196 These multinucleated, tartrate-resistant acid phosphatase-positive cells were positive for recept

197 ly enhanced the number of tartrate-resistant acid phosphatase-positive multinuclear osteoclast-like c

198 by counting the number of tartrate-resistant acid phosphatase-positive multinucleated cells and measu

199 from pannus invasion, and tartrate-resistant acid phosphatase-positive multinucleated cells at sites

200 9, and the generation of tartrate-resistant acid phosphatase-positive multinucleated cells in both c

201 No tartrate-resistant acid phosphatase-positive multinucleated cells or resorp

202 n, forming multinucleated tartrate-resistant acid phosphatase-positive osteoclast-like cells.

203 ctivity was analyzed with tartrate-resistant acid phosphatase-positive osteoclasts and preosteoclasts

204 zed by reduced numbers of tartrate-resistant acid phosphatase-positive osteoclasts at the tumor-bone

205 teoblasts and diminished tartrate resistance acid phosphatase-positive osteoclasts in the defects.

206 The number of tartrate-resistant acid phosphatase-positive osteoclasts was significantly

207 videnced by a decrease in tartrate-resistant acid phosphatase-positive osteoclasts.

208 e marrow macrophages into tartrate-resistant acid phosphatase-positive preosteoclasts in culture but

209 nished formation of TRAP (tartrate-resistant acid phosphatase-positive) multinucleated osteoclasts, a

210 ibited reduced numbers of tartrate-resistant acid-phosphatase-positive cells and more proliferating c

211 bitory compounds for three of the four major acid phosphatases produced by F. tularensis SCHU4: AcpA,

212 d vaccines such as those targeting prostatic acid phosphatase, prostate-specific antigen, and cellula

213 ontaining phosphoesterases, including purple acid phosphatase, protein serine/threonine phosphatases,

214 hosphatase enzymes that also includes purple acid phosphatases, protein phosphatases, and nucleotide

215 Tartrate-resistant acid phosphatase reaction and immunohistochemical staini

216 However, rigorous demonstration of acid phosphatase secretion by intracellular Francisella

217 3.1.3.2), a periplasmic class B nonspecific acid phosphatase, significantly increased activity in pa

218 own to deposphorylate the yeast phosphatidic acid phosphatase Smp2p, and we show that Dullard dephosp

219 A parallel series of tartrate resistant acid phosphatase-stained sections were evaluated for ost

220 teoclasts were counted in tartrate-resistant acid phosphatase-stained sections.

221 assessed via quantitative tartrate-resistant acid phosphatase staining and degradation of human bone

222 ation, adenosine diphosphatase (ADPase), and acid phosphatase staining as well as immunostaining with

223 Tartrate-resistant acid phosphatase staining demonstrated a marked decrease

224 ere expressed widely, and tartrate-resistant acid phosphatase staining notably was absent in the suba

225 On the basis of lysosomal acid phosphatase staining of infected macrophages and A.

226 tomography analysis, and tartrate-resistant acid phosphatase staining revealed reduced trabecular bo

227 Tartrate-resistant acid phosphatase staining was used to identify multinucl

228 with varying intensity of tartrate-resistant acid phosphatase staining were regularly present.

229 H&E and tartrate-resistant acid phosphatase staining were used to characterize and

230 tic cells was assessed by tartrate-resistant acid phosphatase staining, whereas the secretion of matr

231 phages were determined by tartrate-resistant acid phosphatase staining.

232 clasts were enumerated by tartrate-resistant acid phosphatase staining.

233 ells was determined after tartrate-resistant acid phosphatase staining.

234 n to OCs was confirmed by tartrate-resistant acid phosphatase staining; bone resorbing activity was a

235 n maize but greater exudation of citrate and acid phosphatase, suggesting a greater capacity to mobil

236 ificantly reduced their release of secretory acid phosphatases, suggesting that this single thioredox

237 sella spp. is a respiratory-burst-inhibiting acid phosphatase that also exhibits phospholipase C acti

238 M. jannaschii encodes ComB, a Mg2+-dependent acid phosphatase that is specific for 2-hydroxycarboxyli

239 rancisella tularensis contains four putative acid phosphatases that are conserved in Francisella novi

240 nosomes also possess cell-surface-associated acid phosphatases that could play a role in invasion sim

241 nt ectonucleotidase, transmembrane prostatic acid phosphatase (TMPAP), in the SSFP region.

242 hematoxylin and eosin and tartrate-resistant acid phosphatase to confirm the presence of osteolytic b

243 lity of several crystal structures of purple acid phosphatases, to date there is no direct evidence f

244 This is the first evidence of acid phosphatase translocation during macrophage infecti

245 as evidenced by increased tartrate-resistant acid phosphatase (TRAP) activity and multinucleation, wh

246 However, the absence of tartrate-resistant acid phosphatase (TRAP) activity and the lack of F4/80-p

247 inuclear cells expressing tartrate-resistant acid phosphatase (TRAP) activity produced by RANK-L-stim

248 of osteoclastogenesis and tartrate-resistant acid phosphatase (TRAP) activity was evaluated in RANKL-

249 e larger, fail to express tartrate-resistant acid phosphatase (TRAP) activity, and display a propensi

250 gnificantly reduced femur tartrate resistant acid phosphatase (TRAP) activity, suggesting potential r

251 rin-dependent 1 (NFATc1), tartrate-resistant acid phosphatase (TRAP) and cathepsin K in vitro.

252 dia and cell lysates, and tartrate-resistant acid phosphatase (TRAP) and mRNA detection for the osteo

253 ase (AP) for osteoblasts; tartrate-resistant acid phosphatase (TRAP) for osteoclasts; and the mineral

254 , plays a pivotal role in tartrate-resistant acid phosphatase (TRAP) gene expression.

255 gulated by the osteoclast tartrate-resistant acid phosphatase (TRAP) gene promoter (Tg/NCD).

256 ously to the proximal region of the tartrate acid phosphatase (TRAP) gene promoter and suppresses nuc

257 ), osteocalcin (OCN), and tartrate-resistant acid phosphatase (TRAP) immunohistochemical staining wer

258 n-regulates expression of tartrate-resistant acid phosphatase (TRAP) in mature osteoclasts.

259 tion of target genes like tartrate-resistant acid phosphatase (TRAP) in osteoclasts.

260 The tartrate-resistant acid phosphatase (TRAP) is present in multiple tissues,

261 osin and subjected to the tartrate-resistant acid phosphatase (TRAP) method.

262 Tartrate-resistant acid phosphatase (TRAP) plays an important role in bone

263 Tartrate-resistant acid phosphatase (TRAP) staining showed that zoledronate

264 munohistochemistry, using tartrate-resistant acid phosphatase (TRAP) staining to identify osteoclasts

265 Tartrate-resistant acid phosphatase (TRAP) staining, resorption pit assays,

266 istochemical detection of tartrate-resistant acid phosphatase (TRAP) were also performed.

267 steoprotegerin (OPG), and tartrate-resistant acid phosphatase (TRAP) were assessed.

268 ical sections stained for tartrate-resistant acid phosphatase (TRAP) were quantified by histomorphome

269 formation of multinuclear tartrate-resistant acid phosphatase (TRAP)(+) osteoclasts, associated with

270 ), osteoprotegerin (OPG), tartrate-resistant acid phosphatase (TRAP), and activated caspase-3 were pe

271 NK-kappaB ligand (RANKL), tartrate-resistant acid phosphatase (TRAP), and osteoclast-associated recep

272 opeptidase 13 (MMP13) and tartrate-resistant acid phosphatase (TRAP), leading to an acceleration in p

273 ere fixed and stained for tartrate-resistant acid phosphatase (TRAP), Oregon Green 488-phalloidin, a

274 A, the positive cells for tartrate-resistant acid phosphatase (TRAP), receptor activator of nuclear f

275 ion of the active form of tartrate-resistant acid phosphatase (TRAP)-5b.

276 etected the appearance of tartrate-resistant acid phosphatase (TRAP)-negative multinucleated giant (M

277 vel of bone loss and less tartrate-resistant acid phosphatase (TRAP)-positive cell induction than M0

278 ased bone mass, increased tartrate-resistant acid phosphatase (TRAP)-positive cell number, and enhanc

279 rmation of multinucleated tartrate-resistant acid phosphatase (TRAP)-positive cells from primary muri

280 e loss in mice with fewer tartrate-resistant acid phosphatase (TRAP)-positive cells in alveolar bone.

281 ment cells displayed more tartrate-resistant acid phosphatase (TRAP)-positive cells than the co-cultu

282 Tartrate-resistant acid phosphatase (TRAP)-positive osteoclasts in the alve

283 , immunohistochemical, or tartrate-resistant acid phosphatase (TRAP)-stained sections.

284 lars until 6 months using tartrate resistant acid phosphatase (TRAP).

285 steoprotegerin (OPG), and tartrate-resistant acid phosphatase (TRAP).

286 The enzyme tartrate resistant acid phosphatase (TRAP, two isoforms 5a and 5b) is highl

287 , and a decrease in serum tartrate-resistant acid phosphatase (TRAP5b) concentration.

288 Potato acid phosphatase treatment reversibly inactivated the en

289 PhosPhatidic Acid Phosphatase type 2B (PPAP2B), an integral membrane

290 Tartrate-resistant acid phosphatase (type V) (TRAP) was used as the bait in

291 based on rhamnulose-1-phosphate aldolase and acid phosphatase using racemic glyceraldehyde and dihydr

292 S3 and TPSI1 (novel genes); and PAP1 (purple acid phosphatase) was suppressed by Phi in plants and ce

293 kappaB ligand (RANKL) and tartrate resistant acid phosphatase were significantly diminished in CIA-ch

294 lthough levels of type 5b tartrate-resistant acid phosphatase were significantly lower than those obs

295 broad range, phosphate starvation-regulated acid phosphatase, which functionally replaces PHO5 in th

296 F. tularensis subspecies encode a series of acid phosphatases, which have been reported to play impo

297 Francisella spp. encode a variety of acid phosphatases, whose roles in phagosomal escape and

298 MDP-1 is a eukaryotic magnesium-dependent acid phosphatase with little sequence homology to previo

299 An AppA homolog, Agp, a periplasmic acid phosphatase with similar structure, lacks the nonco

300 Lipins are phosphatidic acid phosphatases with a pivotal role in regulation of t